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Jacobs, L. L., Polcyn M. J., Mateus O., Schulp A., Ferguson K., Scotese C., Jacobs B. F., Strganac C., Vineyard D., Myers T. S., & Morais M. L. (2010).  Tectonic Drift, Climate, and Paleoenvironment of Angola Since the Cretaceous. AGU Fall Meeting Abstracts, 1:. 02., Jan Abstractjacobs_polcyn_mateus_et_al_2010_tectonic_drift_climate_and_paleoenvironment_of_angola_since_the_cretaceous.pdf

Africa is the only continent that now straddles arid zones located beneath the descending limbs of both the northern and southern Hadley cells, and it has done so since it became a distinct continent in the Early Cretaceous. Since that time, Africa has drifted tectonically some 12 degrees north and rotated approximately 45 degrees counterclockwise. This changing latitudinal setting and position of the landmass under the relatively stable Hadley Cells is manifested as southward migration of climatic zones over the past 132 million years. Data from kerogen, X-ray diffraction analysis of sedimentary matrix, carbon isotopes from shell samples and tooth enamel,new 40Ar/39Ar radiometric dates, pollen and plant macrofossils, and fossil vertebrates indicate a productive upwelling system adjacent to a coastal desert since the opening of the South Atlantic Ocean; however, the position of the coastal desert has migrated southward as Africa drifted north, resulting in today's Skeleton Coast and Benguela Current. This migration has had a profound effect on the placement of the West African coast relative to areas of high marine productivity and resulting extensive hydrocarbon deposits, on the placement of arid zones relative to the continent especially the Skeleton Coast desert, on the climatic history of the Congo Basin (which shows a Late Cretaceous decrease in aridity based on the relative abundance of analcime in the Samba core), and in reducing the southern temperate region of Africa from 17% of continental area during the Cretaceous to 2% today. We show here that these related geographic and environmental changes drove ecological and evolutionary adjustments in southern African floras and faunas, specifically with respect to the distribution of anthropoid primates, the occurrence of modern relicts such as the gnetalean Welwitschia mirabilis, endemism as in the case of ice plants, and mammalian adaption to an open environment as in springhares. Africa's tectonic drift through climate zones has been a first-order environmental determinant since the Early Cretaceous.

Cunha, P. P., Mateus O., & Antunes M. T. (2004).  The sedimentology of the Paimogo dinosaur nest site (Portugal, Upper Jurassic). 23 rd IAS Meeting of Sedimentology. 93., Coimbra, Portugal Abstractcunha_p_p_2004_-_the_sedimentology_of_the_paimogo_dinosaur_nest_site_portugal10467.pdf

Sedimentological features of the Paimogo site, 6 km NNW of Lourinhã, western central Portugal are presented. More than one hundred theropod dinosaur eggs (some containing embryo bones) ascribed to Lourinhanosaurus antunesi Mateus 1998, three crocodilian eggs and some other fossils were found at the 32 m2 excavated area of the egg-bearing horizon (Mateus et al., 1998). The stratigraphic position of the site is the Praia Azul member (Lourinhã Formation), roughly corresponding to the Kimmeridgian-Tithonian boundary or, more likely lowermost Tithonian. The maximum flooding surface of the basinal transgressive event where the horizon is located corresponds to the base of the H depositional sequence defined by Pena dos Reis et al. (2000) and probably correlates to the base of sequence Ti1 identified within western European basins (Jacquin et al., 1998), dated as 150 Ma. Possibly during the normal river discharge, the theropods congregated in nesting colonies at the backswamp of an extensive flood plain with small meandering channels and freshwater ponds. There are no evidences that the nest was dug or the eggs buried. The eggs have probably been laid on a flat, shaded, muddy area near the bank of a large pond. It is probable that the eggs have not been actively incubated. The larger number of eggs suggest that they were laid near simultaneously by, at least, six females. The fossil record shows that crocodilians, mammals, gastropods and fish were also present. A flood event occurred when theropod embryos had attained a late stade of ontogenetic development, probably just before hatching. The overflow from a nearby channel flooded the plain, including the area where the eggs had been laid. The sheet flood flowing over the nest resulted into the scattering and breaking up of some dinosaur eggs. Eggshell and embryos skeletal parts fragments were displaced to an adjacent area where, due to hydrodynamic decline, the flow submerged other clutches and moderately dragged their eggs. The flooding caused the drowning of the embryos and covered the eggs with fine-grained sediment, hiding them from predators and scavengers. Hydrodynamic interpretation of the arrangement of the theropod eggs and egg-fragments suggests that the flow came from the NW. When the floodwaters receded, the fine-grained deposits became exposed to subaerial weathering. Although the sediment surface was often wet and small bodies of standing water may still have existed, the sediments were oxidized and plant remains have consequently been destroyed. Some carbonate cementation and redenning resulted from pedogenesis under alternating dry and moist conditions, in a semiarid/ sub-tropical climate under seasonal changing, contrasting conditions. The thick, stratigraphically above and below the nesting horizon mudrocks indicate a long persistence of periodic flooding, alternating with pedogenesis. During the early stages of diagenesis, vertical pressure crushed the eggs. Silt penetration into the inner part of each egg inhibited later flattening during the burial process.